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LBF20307PG39 - Revision history
2026-04-30T18:11:16Z
Revision history for this page on the wiki
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Editor at 09:02, 21 October 2010
2010-10-21T09:02:52Z
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<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|SysName=(5-<del style="font-weight: bold; text-decoration: none;">cis,</del>13<del style="font-weight: bold; text-decoration: none;">-trans</del>)-(8R,12S,15R) -15-Hydroxy-9-oxoprost-5,10,13-trienoic acid</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|SysName=(<ins style="font-weight: bold; text-decoration: none;">cis-</ins>5<ins style="font-weight: bold; text-decoration: none;">,trans</ins>-13)-(8R,12S,15R) -15-Hydroxy-9-oxoprost-5,10,13-trienoic acid</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&15-epi Prostaglandin A_2&&(5Z,13E)-(8R,12S,15R) -15-Hydroxy-9-oxoprost-5,10,13-trienoic acid&&</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&15-epi Prostaglandin A_2&&(5Z,13E)-(8R,12S,15R) -15-Hydroxy-9-oxoprost-5,10,13-trienoic acid&&</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra= nu ^{film}_{max}1350 and 970cm^{-1}[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra= nu ^{film}_{max}1350 and 970cm^{-1}[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
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Editor at 06:33, 28 May 2010
2010-05-28T06:33:35Z
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<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (<del style="font-weight: bold; text-decoration: none;">5Z</del>, <del style="font-weight: bold; text-decoration: none;">13E</del>) - (8R,12S,15R) -15-Hydroxy-9-oxoprost-5,10,13-trienoic acid</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|SysName=(<ins style="font-weight: bold; text-decoration: none;">5-cis</ins>,<ins style="font-weight: bold; text-decoration: none;">13-trans</ins>)-(8R,12S,15R) -15-Hydroxy-9-oxoprost-5,10,13-trienoic acid</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&15-epi Prostaglandin A_2&&</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&15-epi Prostaglandin A_2<ins style="font-weight: bold; text-decoration: none;">&&(5Z,13E)-(8R,12S,15R) -15-Hydroxy-9-oxoprost-5,10,13-trienoic acid</ins>&&</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra= nu ^{film}_{max}1350 and 970cm^{-1}[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra= nu ^{film}_{max}1350 and 970cm^{-1}[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H-NMR delta ppm5.41, 5.58.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H-NMR delta ppm5.41, 5.58.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
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Editor at 05:40, 23 April 2010
2010-04-23T05:40:45Z
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidMaps=LMFA03010092</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidMaps=LMFA03010092</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (5Z, 13E) - (8R,12S,15R) -15-<del style="font-weight: bold; text-decoration: none;">hydroxy</del>-9-oxoprost-5,10,13-trienoic acid</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (5Z, 13E) - (8R,12S,15R) -15-<ins style="font-weight: bold; text-decoration: none;">Hydroxy</ins>-9-oxoprost-5,10,13-trienoic acid</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&15-epi<del style="font-weight: bold; text-decoration: none;">-prostaglandin </del>A_2&&</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&15-epi <ins style="font-weight: bold; text-decoration: none;">Prostaglandin </ins>A_2&&</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra= nu ^{film}_{max}1350 and 970cm^{-1}[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra= nu ^{film}_{max}1350 and 970cm^{-1}[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H-NMR delta ppm5.41, 5.58.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H-NMR delta ppm5.41, 5.58.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
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Editor at 21:00, 14 April 2010
2010-04-14T21:00:00Z
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (5Z, 13E) - (8R,12S,15R) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (5Z, 13E) - (8R,12S,15R) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&15-epi-prostaglandin A_2<del style="font-weight: bold; text-decoration: none;">&&(5Z, 13E) - (8R,12S,15R) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid</del>&&</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&15-epi-prostaglandin A_2&&</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra= nu ^{film}_{max}1350 and 970cm^{-1}[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra= nu ^{film}_{max}1350 and 970cm^{-1}[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H-NMR delta ppm5.41, 5.58.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H-NMR delta ppm5.41, 5.58.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
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Editor at 10:00, 25 February 2010
2010-02-25T10:00:10Z
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (5Z, 13E) - (8R,12S,15R) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (5Z, 13E) - (8R,12S,15R) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&15-epi-prostaglandin A_2&&(5Z, 13E) - (8R,12S,15R) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid&&</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&15-epi-prostaglandin A_2&&(5Z, 13E) - (8R,12S,15R) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid&&</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra= nu ^<del style="font-weight: bold; text-decoration: none;">f_m _a _x </del>1350 and 970cm^- <del style="font-weight: bold; text-decoration: none;">^</del>1 [[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra= nu ^<ins style="font-weight: bold; text-decoration: none;">{film}_{max}</ins>1350 and 970cm^<ins style="font-weight: bold; text-decoration: none;">{</ins>-1<ins style="font-weight: bold; text-decoration: none;">}</ins>[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H-NMR delta ppm5.41, 5.58.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H-NMR delta ppm5.41, 5.58.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=15-Epi-prostaglandin A _2 and its acetate methyl ester were isolated from Caribbean Gorgonian, Plexaura homomalla.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=15-Epi-prostaglandin A _2 and its acetate methyl ester were isolated from Caribbean Gorgonian, Plexaura homomalla.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
</table>
Editor
https://lipidbank.jp/mediawiki/index.php?title=LBF20307PG39&diff=53974&oldid=prev
Editor at 14:00, 19 February 2010
2010-02-19T14:00:10Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 23:00, 19 February 2010</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (5Z, 13E) - (8R,12S,15R) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (5Z, 13E) - (8R,12S,15R) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&15-epi-prostaglandin A_2&&(5Z, 13E) - (8R,12S,15R) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid&&</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&15-epi-prostaglandin A_2&&(5Z, 13E) - (8R,12S,15R) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid&&</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra=nu^f_m _a _x 1350 and 970cm^- ^1 [[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra= nu ^f_m _a _x 1350 and 970cm^- ^1 [[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H-<del style="font-weight: bold; text-decoration: none;">NMRdeltappm5</del>.41, 5.58.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H-<ins style="font-weight: bold; text-decoration: none;">NMR delta ppm5</ins>.41, 5.58.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=15-Epi-prostaglandin A _2 and its acetate methyl ester were isolated from Caribbean Gorgonian, Plexaura homomalla.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=15-Epi-prostaglandin A _2 and its acetate methyl ester were isolated from Caribbean Gorgonian, Plexaura homomalla.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chemical Synthesis=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chemical Synthesis=</div></td></tr>
</table>
Editor
https://lipidbank.jp/mediawiki/index.php?title=LBF20307PG39&diff=53973&oldid=prev
Editor at 14:00, 19 February 2010
2010-02-19T14:00:00Z
<p></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 23:00, 19 February 2010</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (5Z, 13E) - (8R,12S,15R) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (5Z, 13E) - (8R,12S,15R) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&15-epi-prostaglandin A_2&&(5Z, 13E) - (8R,12S,15R) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid&&</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&15-epi-prostaglandin A_2&&(5Z, 13E) - (8R,12S,15R) -15-hydroxy-9-oxoprost-5,10,13-trienoic acid&&</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra=<del style="font-weight: bold; text-decoration: none;"><FONT FACE="Symbol">n</FONT><SUP><FONT SIZE=-1>f</FONT></SUP><SUP><FONT SIZE=-1>i</FONT></SUP><SUP><FONT SIZE=-1>l</FONT></SUP><SUP><FONT SIZE=-1>m</FONT></SUP><SUB><FONT SIZE=-1>m</FONT></SUB><SUB><FONT SIZE=-1>a</FONT></SUB><SUB><FONT SIZE=-1>x</FONT></SUB></del>1350 and 970cm<del style="font-weight: bold; text-decoration: none;"><SUP><FONT SIZE=</del>-1<del style="font-weight: bold; text-decoration: none;">>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP></del>[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra=<ins style="font-weight: bold; text-decoration: none;">nu^f_m _a _x </ins>1350 and 970cm<ins style="font-weight: bold; text-decoration: none;">^</ins>- <ins style="font-weight: bold; text-decoration: none;">^</ins>1 [[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=<del style="font-weight: bold; text-decoration: none;"><SUP><FONT SIZE=-1></del>1<del style="font-weight: bold; text-decoration: none;"></FONT></SUP></del>H-<del style="font-weight: bold; text-decoration: none;">NMR<FONT FACE="Symbol">d</FONT>ppm5</del>.41, 5.58.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=<ins style="font-weight: bold; text-decoration: none;">^</ins>1 H-<ins style="font-weight: bold; text-decoration: none;">NMRdeltappm5</ins>.41, 5.58.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Source=15-Epi-prostaglandin A <del style="font-weight: bold; text-decoration: none;"><SUB><FONT SIZE=-1>2</FONT></SUB> </del>and its acetate methyl ester were isolated from Caribbean Gorgonian, Plexaura homomalla.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Source=15-Epi-prostaglandin A <ins style="font-weight: bold; text-decoration: none;">_2 </ins>and its acetate methyl ester were isolated from Caribbean Gorgonian, Plexaura homomalla.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chemical Synthesis=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chemical Synthesis=</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Metabolism=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Metabolism=</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Symbol=(15R)-<del style="font-weight: bold; text-decoration: none;">PGA<SUB><FONT SIZE=-1>2</FONT></SUB></del></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Symbol=(15R)-<ins style="font-weight: bold; text-decoration: none;">PGA_2 </ins></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>}}</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>}}</div></td></tr>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Lipid/Footer}}</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Lipid/Footer}}</div></td></tr>
</table>
Editor
https://lipidbank.jp/mediawiki/index.php?title=LBF20307PG39&diff=53972&oldid=prev
Editor at 21:00, 6 January 2010
2010-01-06T21:00:00Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 06:00, 7 January 2010</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Metabolism=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Metabolism=</div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">|Symbol=(15R)-PGA<SUB><FONT SIZE=-1>2</FONT></SUB></ins></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>}}</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>}}</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Lipid/Footer}}</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Lipid/Footer}}</div></td></tr>
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Editor
https://lipidbank.jp/mediawiki/index.php?title=LBF20307PG39&diff=53971&oldid=prev
Editor at 11:55, 25 November 2009
2009-11-25T11:55:00Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:55, 25 November 2009</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra=<FONT FACE="Symbol">n</FONT><SUP><FONT SIZE=-1>f</FONT></SUP><SUP><FONT SIZE=-1>i</FONT></SUP><SUP><FONT SIZE=-1>l</FONT></SUP><SUP><FONT SIZE=-1>m</FONT></SUP><SUB><FONT SIZE=-1>m</FONT></SUB><SUB><FONT SIZE=-1>a</FONT></SUB><SUB><FONT SIZE=-1>x</FONT></SUB>1350 and 970cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra=<FONT FACE="Symbol">n</FONT><SUP><FONT SIZE=-1>f</FONT></SUP><SUP><FONT SIZE=-1>i</FONT></SUP><SUP><FONT SIZE=-1>l</FONT></SUP><SUP><FONT SIZE=-1>m</FONT></SUP><SUB><FONT SIZE=-1>m</FONT></SUB><SUB><FONT SIZE=-1>a</FONT></SUB><SUB><FONT SIZE=-1>x</FONT></SUB>1350 and 970cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR<FONT FACE="Symbol">d</FONT>ppm5.41, 5.58.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR<FONT FACE="Symbol">d</FONT>ppm5.41, 5.58.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Source=15-Epi-prostaglandin A <SUB><FONT SIZE=-1>2</FONT></SUB> and its acetate methyl ester were isolated from Caribbean Gorgonian, Plexaura homomalla.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]<del style="font-weight: bold; text-decoration: none;">;></del></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Source=15-Epi-prostaglandin A <SUB><FONT SIZE=-1>2</FONT></SUB> and its acetate methyl ester were isolated from Caribbean Gorgonian, Plexaura homomalla.[[Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185|{{RelationTable/GetFirstAuthor|Reference:Weinheimer_AJ:Spraggins_RL:,Tetrahedron Lett.,1969,59,5185}}]]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chemical Synthesis=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chemical Synthesis=</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Metabolism=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Metabolism=</div></td></tr>
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Editor
https://lipidbank.jp/mediawiki/index.php?title=LBF20307PG39&diff=53970&oldid=prev
Editor at 10:00, 25 November 2009
2009-11-25T10:00:00Z
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<td colspan="1" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="1" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 19:00, 25 November 2009</td>
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